Medical Device Manufacturer · US , Bedford , OH

Brainmaster Technologies, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2016

Total

Cleared

Denied

Brainmaster Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in Bedford, US.

Historical record: 2 cleared submissions from 2016 to 2018. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Brainmaster Technologies, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Brainmaster Technologies, Inc.

2 devices

1-2 of 2